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Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity

Poly(ADP-ribosyl)ation is a reversible post-translational modification synthetized by ADP-ribose transferases and removed by poly(ADP-ribose) glycohydrolase (PARG), which plays important roles in DNA damage repair. While well-studied in somatic tissues, much less is known about poly(ADP-ribosyl)atio...

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Autores principales: Janisiw, Eva, Raices, Marilina, Balmir, Fabiola, Paulin, Luis F., Baudrimont, Antoine, von Haeseler, Arndt, Yanowitz, Judith L., Jantsch, Verena, Silva, Nicola
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519143/
https://www.ncbi.nlm.nih.gov/pubmed/32978394
http://dx.doi.org/10.1038/s41467-020-18693-1
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author Janisiw, Eva
Raices, Marilina
Balmir, Fabiola
Paulin, Luis F.
Baudrimont, Antoine
von Haeseler, Arndt
Yanowitz, Judith L.
Jantsch, Verena
Silva, Nicola
author_facet Janisiw, Eva
Raices, Marilina
Balmir, Fabiola
Paulin, Luis F.
Baudrimont, Antoine
von Haeseler, Arndt
Yanowitz, Judith L.
Jantsch, Verena
Silva, Nicola
author_sort Janisiw, Eva
collection PubMed
description Poly(ADP-ribosyl)ation is a reversible post-translational modification synthetized by ADP-ribose transferases and removed by poly(ADP-ribose) glycohydrolase (PARG), which plays important roles in DNA damage repair. While well-studied in somatic tissues, much less is known about poly(ADP-ribosyl)ation in the germline, where DNA double-strand breaks are introduced by a regulated program and repaired by crossover recombination to establish a tether between homologous chromosomes. The interaction between the parental chromosomes is facilitated by meiotic specific adaptation of the chromosome axes and cohesins, and reinforced by the synaptonemal complex. Here, we uncover an unexpected role for PARG in coordinating the induction of meiotic DNA breaks and their homologous recombination-mediated repair in Caenorhabditis elegans. PARG-1/PARG interacts with both axial and central elements of the synaptonemal complex, REC-8/Rec8 and the MRN/X complex. PARG-1 shapes the recombination landscape and reinforces the tightly regulated control of crossover numbers without requiring its catalytic activity. We unravel roles in regulating meiosis, beyond its enzymatic activity in poly(ADP-ribose) catabolism.
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spelling pubmed-75191432020-10-14 Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity Janisiw, Eva Raices, Marilina Balmir, Fabiola Paulin, Luis F. Baudrimont, Antoine von Haeseler, Arndt Yanowitz, Judith L. Jantsch, Verena Silva, Nicola Nat Commun Article Poly(ADP-ribosyl)ation is a reversible post-translational modification synthetized by ADP-ribose transferases and removed by poly(ADP-ribose) glycohydrolase (PARG), which plays important roles in DNA damage repair. While well-studied in somatic tissues, much less is known about poly(ADP-ribosyl)ation in the germline, where DNA double-strand breaks are introduced by a regulated program and repaired by crossover recombination to establish a tether between homologous chromosomes. The interaction between the parental chromosomes is facilitated by meiotic specific adaptation of the chromosome axes and cohesins, and reinforced by the synaptonemal complex. Here, we uncover an unexpected role for PARG in coordinating the induction of meiotic DNA breaks and their homologous recombination-mediated repair in Caenorhabditis elegans. PARG-1/PARG interacts with both axial and central elements of the synaptonemal complex, REC-8/Rec8 and the MRN/X complex. PARG-1 shapes the recombination landscape and reinforces the tightly regulated control of crossover numbers without requiring its catalytic activity. We unravel roles in regulating meiosis, beyond its enzymatic activity in poly(ADP-ribose) catabolism. Nature Publishing Group UK 2020-09-25 /pmc/articles/PMC7519143/ /pubmed/32978394 http://dx.doi.org/10.1038/s41467-020-18693-1 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Janisiw, Eva
Raices, Marilina
Balmir, Fabiola
Paulin, Luis F.
Baudrimont, Antoine
von Haeseler, Arndt
Yanowitz, Judith L.
Jantsch, Verena
Silva, Nicola
Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity
title Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity
title_full Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity
title_fullStr Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity
title_full_unstemmed Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity
title_short Poly(ADP-ribose) glycohydrolase coordinates meiotic DNA double-strand break induction and repair independent of its catalytic activity
title_sort poly(adp-ribose) glycohydrolase coordinates meiotic dna double-strand break induction and repair independent of its catalytic activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7519143/
https://www.ncbi.nlm.nih.gov/pubmed/32978394
http://dx.doi.org/10.1038/s41467-020-18693-1
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